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Summary Literature (0)
MIM:188050 - THROMBOPHILIA DUE TO THROMBIN DEFECT; THPH1

Xenbase Genes: habp2, mthfr, f2, f13a1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008559 - thrombophilia due to thrombin defect

Disease Ontology (DO):
DOID:0080701 - prothrombin thrombophilia
DOID:0111907 - thrombophilia due to thrombin defect
DOID:2452 - thrombophilia